Demo Data from EDBT 2026 / reviewers in the wild / expert
David Israeli
dblp:150/1342
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2014
0000-0003-2762-2195ORCID · reported
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 2 heaviest of 2, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › kernel methods
multiple kernel learning |
0.2 | 1 | 2014 | Towards a piRNA prediction using multiple kernel fusion and support vector machine · Bioinform. 2014 |
Bioinformatics and computational biology › transcriptomics
non-coding RNA analysis |
0.1 | 1 | 2014 | Towards a piRNA prediction using multiple kernel fusion and support vector machine · Bioinform. 2014 |
Methods — techniques the papers use, named apart from their topics
support vector machine · 0.2multiple kernel fusion · 0.2
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2014 | Towards a piRNA prediction using multiple kernel fusion and support vector machineabstractMOTIVATION: Piwi-interacting RNA (piRNA) is the most recently discovered and the least investigated class of Argonaute/Piwi protein-interacting small non-coding RNAs. The piRNAs are mostly known to be involved in protecting the genome from invasive transposable elements. But recent discoveries suggest their involvement in the pathophysiology of diseases, such as cancer. Their identification is therefore an important task, and computational methods are needed. However, the lack of conserved piRNA sequences and structural elements makes this identification challenging and difficult. RESULTS: In the present study, we propose a new modular and extensible machine learning method based on multiple kernels and a support vector machine (SVM) classifier for piRNA identification. Very few piRNA features are known to date. The use of a multiple kernels approach allows editing, adding or removing piRNA features that can be heterogeneous in a modular manner according to their relevance in a given species. Our algorithm is based on a combination of the previously identified features [sequence features (k-mer motifs and a uridine at the first position) and piRNAs cluster feature] and a new telomere/centromere vicinity feature. These features are heterogeneous, and the kernels allow to unify their representation. The proposed algorithm, named piRPred, gives promising results on Drosophila and Human data and outscores previously published piRNA identification algorithms. AVAILABILITY AND IMPLEMENTATION: piRPred is freely available to non-commercial users on our Web server EvryRNA http://EvryRNA.ibisc.univ-evry.fr. Jocelyn Brayet, Farida Zehraoui, Laurence Jeanson-Leh, David Israeli, Fariza Tahi |
Bioinform. | 4 |